Label: THERA DERM ROLL ON- methyl salicylate liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated February 19, 2018

If you are a consumer or patient please visit this version.

  • DOSAGE & ADMINISTRATION

    Theraderm Roll on is to be used on sore muscles, for minor aches and pains. If pain persists for more than three days consult your doctor.Apply small amount onto affected area and repeat three (3) to four (4) times daily.

  • INDICATIONS & USAGE

    For the relief of minor aches and pains, muscles aches or sprains, and minor back or arthritis pain.

  • Warning: For External Use Only

    Use only as directed. Avoid contact with the eyes and mucous membranes. Do not apply to wounds, damaged or very sensitive skin. Test on a small area before use. DO not use in combination with other analgesic products.DO not bandage tightly or cover with any type of wrap except clothing. If condition worsens, or persists for more than seven days, discontinue use and consult a physician.

  • Keep out of the Reach of Children

    If swallowed,get medical help or contact Poision Control right away.

  • Active Ingredients:

    Menthol Natural

    Methyl Salicilate

    Peppermint oil

    Menthol Crystal

  • Inactive Ingredients:

    Aloe extract, Vitamin E Oil ,Lavender Flos,Angelicae Sinesis Rx, Cauda,Salviae,Miltiorrhiza, Chuanxiong, Paeoniae Rubra, Frakinsense, Mrryha, Carthami Flos, Persicae Sm, Cordalis Rz, Nototerygium, Incisum, and Angelica Pubescentis Rx.

  • PURPOSE

    For the relief of minor aches and pains, related to strains and sprains and minor injury.

  • Theraderm Roll on

    Label Roll On

  • INGREDIENTS AND APPEARANCE
    THERA DERM ROLL ON 
    methyl salicylate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:16903-171
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    METHYL SALICYLATE 2-ETHYLBUTYRATE (UNII: J8D9175Q0G) (METHYL SALICYLATE 2-ETHYLBUTYRATE - UNII:J8D9175Q0G) METHYL SALICYLATE 2-ETHYLBUTYRATE18 mg  in 90 mg
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)4 mg  in 90 mg
    PEPPERMINT OIL (UNII: AV092KU4JH) (PEPPERMINT - UNII:V95R5KMY2B) PEPPERMINT OIL9 mg  in 90 mg
    MENTHOL 1-PROPYLENE GLYCOL CARBONATE, (-)- (UNII: 2WL8FX4EEZ) (MENTHOL 1-PROPYLENE GLYCOL CARBONATE, (-)- - UNII:2WL8FX4EEZ) MENTHOL 1-PROPYLENE GLYCOL CARBONATE, (-)-9 mg  in 90 mg
    Inactive Ingredients
    Ingredient NameStrength
    PRUNUS PERSICA FLOWER BUD (UNII: 8S5Y7XFT0F) 2 mg  in 90 mg
    NOTOPTERYGIUM FRANCHETII ROOT (UNII: KRT28P6ITK) 2 mg  in 90 mg
    ANGELICA PUBESCENS ROOT (UNII: 0MF1EI01KJ) 2 mg  in 90 mg
    ZINGIBER CASSUMUNAR ROOT OIL (UNII: O47HX41O6C) 2 mg  in 90 mg
    MYRRH (UNII: JC71GJ1F3L) 2 mg  in 90 mg
    ALOE (UNII: V5VD430YW9) 2 mg  in 90 mg
    SALVIA MILTIORRHIZA ROOT (UNII: 1693AM5SBN) 2 mg  in 90 mg
    CARTHAMUS TINCTORIUS FLOWER OIL (UNII: SDQ136WIM5) 2 mg  in 90 mg
    LAVENDER OIL (UNII: ZBP1YXW0H8) 1 mg  in 90 mg
    ANGELICA SINENSIS ROOT (UNII: B66F4574UG) 2 mg  in 90 mg
    LIGUSTICUM SINENSE SUBSP. CHUANXIONG ROOT (UNII: RR83T99U97) 2 mg  in 90 mg
    FRANKINCENSE OIL (UNII: 67ZYA5T02K) 2 mg  in 90 mg
    STEARIC ACID (UNII: 4ELV7Z65AP) 5 mg  in 90 mg
    PHENOXYETHANOL (UNII: HIE492ZZ3T) 1 mg  in 90 mg
    COCONUT OIL (UNII: Q9L0O73W7L) 2 mg  in 90 mg
    Product Characteristics
    Colorwhite (Smooth Non -greasy Roll On) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:16903-171-0490 mg in 1 BOTTLE; Type 0: Not a Combination Product07/31/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/31/2017
    Labeler - Manna Omni International Incorporated (019109468)